QTL Analysis of Head Splitting Resistance in Cabbage (Brassica oleracea L. var. capitata) Using SSR and InDel Makers Based on Whole-Genome Re-Sequencing

PLoS One. 2015 Sep 25;10(9):e0138073. doi: 10.1371/journal.pone.0138073. eCollection 2015.

Abstract

Head splitting resistance (HSR) in cabbage is an important trait closely related to both quality and yield of head. However, the genetic control of this trait remains unclear. In this study, a doubled haploid (DH) population derived from an intra-cross between head splitting-susceptible inbred cabbage line 79-156 and resistant line 96-100 was obtained and used to analyze inheritance and detect quantitative trait loci (QTLs) for HSR using a mixed major gene/polygene inheritance analysis and QTL mapping. HSR can be attributed to additive-epistatic effects of three major gene pairs combined with those of polygenes. Negative and significant correlations were also detected between head Hsr and head vertical diameter (Hvd), head transverse diameter (Htd) and head weight (Hw). Using the DH population, a genetic map was constructed with simple sequence repeat (SSR) and insertion-deletion (InDel) markers, with a total length of 1065.9 cM and average interval length of 4.4 cM between adjacent markers. Nine QTLs for HSR were located on chromosomes C3, C4, C7, and C9 based on 2 years of phenotypic data using both multiple-QTL mapping and inclusive composite interval mapping. The identified QTLs collectively explained 39.4 to 59.1% of phenotypic variation. Three major QTLs (Hsr 3.2, 4.2, 9.2) showing a relatively larger effect were robustly detected in different years or with different mapping methods. The HSR trait was shown to have complex genetic mechanisms. Results from QTL mapping and classical genetic analysis were consistent. The QTLs obtained in this study should be useful for molecular marker-assisted selection in cabbage breeding and provide a foundation for further research on HSR genetic regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brassica / genetics*
  • Chromosomes, Plant / genetics*
  • Genome, Plant*
  • Genome-Wide Association Study
  • High-Throughput Nucleotide Sequencing
  • INDEL Mutation*
  • Plant Breeding
  • Quantitative Trait Loci*

Grants and funding

This work was supported by the National High Technology Research and Development Program (863 Program) of China (2012AA100104, 2012AA100105), the Key Projects in the National Science and Technology Pillar Program of China (2013BAD01B04), the China Agriculture Research System (CARS-25-A), the Key Laboratory of Biology and Genetic Improvement of Horticultural Crops, Ministry of Agriculture, People’s Republic of China, the Science and Technology Innovation Program of the Chinese Academy of Agricultural Sciences (Grant no. CAAS-ASTIP-IVFCAAS). YML received all the funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.